Departamento de Farmacologia, Universidade Federal de Santa Catarina, Florianópolis, SC, Brazil.
J Alzheimers Dis. 2012;32(2):495-511. doi: 10.3233/JAD-2012-120541.
There is increasing evidence that hypercholesterolemia during midlife may represent a predictor of subsequent mild cognitive impairments and dementia decades later. However, the exact mechanism underlying this phenomenon remains unknown since plasmatic cholesterol is not able to cross the blood-brain barrier. In the present study, we evaluated the hypothesis that cognitive impairments triggered by hypercholesterolemia during aging may be related to brain oxidative stress and altered brain acetylcholinesterase (AChE) activity. We also performed a neuropathological investigation in order to analyze whether the cognitive impairments may be associated with stroke-related features. To address these questions we used three- and fourteen-month-old low-density lipoprotein receptor-deficient mice (LDLr-/-). The current findings provide new evidence that aged LDLr-/- mice, exposed to over three-fold cholesterol levels from early life, show working, spatial reference, and procedural memory impairments, without alterations in motor function. Antioxidant imbalance and oxidative damage were evidenced by a marked increase in lipid peroxidation (thiobarbituric acid reactive substances levels) and glutathione metabolism (increase in glutathione levels, glutathione reductase, and glutathione peroxidase activities) together with a significant increase in the AChE activity in the prefrontal cortex of aged hypercholesterolemic LDLr-/- mice. Notably, hypercholesterolemia was not related to brain infarcts and neurodegeneration in mice, independent of their age. These observations provide new evidence that hypercholesterolemia during aging triggers cognitive impairments on different types of learning and memory, accompanied by antioxidant imbalance, oxidative damage, and alterations of cholinergic signaling in brain areas associated with learning and memory processes, particularly in the prefrontal cortex.
越来越多的证据表明,中年时期的高胆固醇血症可能是数十年后出现轻度认知障碍和痴呆的预测因素。然而,由于血浆胆固醇无法穿过血脑屏障,因此这种现象的确切机制尚不清楚。在本研究中,我们评估了这样一种假设,即衰老过程中高胆固醇血症引发的认知障碍可能与大脑氧化应激和乙酰胆碱酯酶(AChE)活性改变有关。我们还进行了神经病理学研究,以分析认知障碍是否与与中风相关的特征有关。为了解决这些问题,我们使用了三个月和十四个月大的低密度脂蛋白受体缺陷型小鼠(LDLr-/-)。目前的研究结果提供了新的证据,表明从早期生活中暴露于三倍以上胆固醇水平的老年 LDLr-/- 小鼠表现出工作记忆、空间参考记忆和程序记忆障碍,而运动功能没有改变。抗氧化失衡和氧化损伤的证据是脂质过氧化(硫代巴比妥酸反应物质水平)和谷胱甘肽代谢(谷胱甘肽水平增加、谷胱甘肽还原酶和谷胱甘肽过氧化物酶活性增加)明显增加,以及 AChE 活性在前额叶皮层中的显著增加在老年高胆固醇血症 LDLr-/- 小鼠中。值得注意的是,高胆固醇血症与小鼠的脑梗死和神经退行性变无关,无论其年龄大小。这些观察结果提供了新的证据,表明衰老过程中的高胆固醇血症会引发不同类型的学习和记忆认知障碍,伴随着抗氧化失衡、氧化损伤和与学习和记忆过程相关的大脑区域胆碱能信号的改变,特别是在前额叶皮层。